US4977115A - Thixotropic refractory material and a process and apparatus for lining metallurgical vessels with this material by a vibration method - Google Patents
Thixotropic refractory material and a process and apparatus for lining metallurgical vessels with this material by a vibration method Download PDFInfo
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- US4977115A US4977115A US06/902,354 US90235486A US4977115A US 4977115 A US4977115 A US 4977115A US 90235486 A US90235486 A US 90235486A US 4977115 A US4977115 A US 4977115A
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- 239000000463 material Substances 0.000 title claims abstract description 34
- 239000011819 refractory material Substances 0.000 title claims abstract description 21
- 238000000034 method Methods 0.000 title claims abstract description 19
- 230000009974 thixotropic effect Effects 0.000 title claims abstract description 13
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 claims abstract description 29
- 239000002245 particle Substances 0.000 claims description 25
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 18
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 14
- 239000000126 substance Substances 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 11
- 229910052593 corundum Inorganic materials 0.000 claims description 10
- 239000010431 corundum Substances 0.000 claims description 10
- 229910052910 alkali metal silicate Inorganic materials 0.000 claims description 7
- 229910052782 aluminium Inorganic materials 0.000 claims description 7
- 239000000377 silicon dioxide Substances 0.000 claims description 7
- 238000001228 spectrum Methods 0.000 claims description 7
- DHAHRLDIUIPTCJ-UHFFFAOYSA-K aluminium metaphosphate Chemical compound [Al+3].[O-]P(=O)=O.[O-]P(=O)=O.[O-]P(=O)=O DHAHRLDIUIPTCJ-UHFFFAOYSA-K 0.000 claims description 6
- 238000004458 analytical method Methods 0.000 claims description 5
- 239000004568 cement Substances 0.000 claims description 4
- 239000004927 clay Substances 0.000 claims description 4
- 229910052700 potassium Inorganic materials 0.000 claims description 4
- 239000011164 primary particle Substances 0.000 claims description 4
- 239000000080 wetting agent Substances 0.000 claims description 4
- 239000003963 antioxidant agent Substances 0.000 claims description 3
- 230000003078 antioxidant effect Effects 0.000 claims description 2
- 239000008119 colloidal silica Substances 0.000 claims 1
- 229910000831 Steel Inorganic materials 0.000 abstract description 18
- 239000010959 steel Substances 0.000 abstract description 18
- 150000001875 compounds Chemical class 0.000 description 13
- 238000002156 mixing Methods 0.000 description 11
- 229910052681 coesite Inorganic materials 0.000 description 6
- 229910052906 cristobalite Inorganic materials 0.000 description 6
- 239000002893 slag Substances 0.000 description 6
- 229910052682 stishovite Inorganic materials 0.000 description 6
- 229910052905 tridymite Inorganic materials 0.000 description 6
- 239000000155 melt Substances 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 230000035699 permeability Effects 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- 229910018404 Al2 O3 Inorganic materials 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000004115 Sodium Silicate Substances 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- 230000008595 infiltration Effects 0.000 description 2
- 238000001764 infiltration Methods 0.000 description 2
- 229910052748 manganese Inorganic materials 0.000 description 2
- 239000011572 manganese Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000010079 rubber tapping Methods 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 229910052911 sodium silicate Inorganic materials 0.000 description 2
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- MXRIRQGCELJRSN-UHFFFAOYSA-N O.O.O.[Al] Chemical compound O.O.O.[Al] MXRIRQGCELJRSN-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical group [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- ZPUCINDJVBIVPJ-LJISPDSOSA-N cocaine Chemical compound O([C@H]1C[C@@H]2CC[C@@H](N2C)[C@H]1C(=O)OC)C(=O)C1=CC=CC=C1 ZPUCINDJVBIVPJ-LJISPDSOSA-N 0.000 description 1
- 238000005056 compaction Methods 0.000 description 1
- 238000012926 crystallographic analysis Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005429 filling process Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011856 silicon-based particle Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000000161 steel melt Substances 0.000 description 1
- 230000032258 transport Effects 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Images
Classifications
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/626—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
- C04B35/63—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B using additives specially adapted for forming the products, e.g.. binder binders
- C04B35/6303—Inorganic additives
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
- C04B35/48—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on zirconium or hafnium oxides, zirconates, zircon or hafnates
- C04B35/481—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on zirconium or hafnium oxides, zirconates, zircon or hafnates containing silicon, e.g. zircon
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/66—Monolithic refractories or refractory mortars, including those whether or not containing clay
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F27—FURNACES; KILNS; OVENS; RETORTS
- F27D—DETAILS OR ACCESSORIES OF FURNACES, KILNS, OVENS OR RETORTS, IN SO FAR AS THEY ARE OF KINDS OCCURRING IN MORE THAN ONE KIND OF FURNACE
- F27D1/00—Casings; Linings; Walls; Roofs
- F27D1/0003—Linings or walls
- F27D1/0006—Linings or walls formed from bricks or layers with a particular composition or specific characteristics
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/00034—Physico-chemical characteristics of the mixtures
- C04B2111/0012—Thixotropic mixtures
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3217—Aluminum oxide or oxide forming salts thereof, e.g. bauxite, alpha-alumina
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3231—Refractory metal oxides, their mixed metal oxides, or oxide-forming salts thereof
- C04B2235/3244—Zirconium oxides, zirconates, hafnium oxides, hafnates, or oxide-forming salts thereof
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/34—Non-metal oxides, non-metal mixed oxides, or salts thereof that form the non-metal oxides upon heating, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3418—Silicon oxide, silicic acids or oxide forming salts thereof, e.g. silica sol, fused silica, silica fume, cristobalite, quartz or flint
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/34—Non-metal oxides, non-metal mixed oxides, or salts thereof that form the non-metal oxides upon heating, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/349—Clays, e.g. bentonites, smectites such as montmorillonite, vermiculites or kaolines, e.g. illite, talc or sepiolite
Definitions
- thixotropy whereby the materials become liquid when subjected to vibrations and are converted to a solid state when the vibration ends, is utilised for lining metallurgical vessels with vibration of the lining material.
- This lining technique has been introduced into the steel industry for lining tapping spouts in blast furnaces.
- the thixotropic refractory material is introduced into the tapping spout, caused to flow with the aid of a vibration template, and homogenised and compacted.
- the density of the refractory thixotropic compound used is important with regard to the slag resistance of the refractory lining. Specialists have hitherto apparently been of the opinion that, in the case of ladles in steel plants, an adequate density of the refractory lining cannot be achieved by vibration.
- the compound disclosed as a refractory compound for lining ladles in steel plants is a pourable compound whose principal components are zirconium silicate, a siliceous raw material, for example fireclay, and an alumina binder, the total alumina content of the pourable material being restricted to 5-1.0% by weight (German Auslegeschrift No. 3,235,244, and Nippon Kokan Technical Report, Overseas No. 37, 1983, pages 51 to 53).
- a disadvantage is the relatively high porosity of 16.5 to 21.5 vol. % and the consequent insufficient slag resistance owing to greater infiltration.
- the lining tends to shrink and is consequently susceptible to fracture.
- the compound contains water of crystallisation. It also contains free SiO 2 . This is disadvantageous because SiO 2 is reduced in the presence of manganese-containing melts, and siliconisation of the steel occurs.
- U.S. Pat. No. 4,292,084 discloses a refractory material for lining metallurgical vessels by vibrating the material to compact it, which can consist of zirconium silicate, tabular alumina, calcined kaolin and phosphoric acid.
- the intention is to improve the infiltration-resistance and slag-repellant action of the lining, as well as its stability under load.
- a thixotropic self-curing refractory material based on zirconium silicate having the following chemical composition (in % by weight):
- the refractory material should preferably have the following crystallographic analysis (in % by weight):
- Molar ratio is the ratio of the alkali metals to the silicate part of alkali metal silicates.
- the zirconium silicate should preferably have the following particle size spectrum:
- the fused product should preferably possess a bulk density of at least 3.60 g/cm 3 and a total porosity of 8% or less.
- the alumina used should preferably be reactive ⁇ -alumina which has a mean primary particle size of less than 3.5 ⁇ m and in which at least 45% of the particles have a size of less than 2 ⁇ m.
- antioxidants preferably in the form of aluminum and/or silicon particles, can be added to the material.
- pulverulent wetting agents preferably alkyl-aryl-polyoxyethanol, which reduce the surface tension of the water for mixing.
- the amount added is 0.05 to 0.2% by weight.
- a further object of the invention is to propose a suitable process and an apparatus for lining metallurgical vessels, with the thixotropic refractory material according to the invention by a vibration method.
- the components of the material in the dry state are first mixed thoroughly. Water is added and the wetted material is mixed again. The material is then introduced under continuous vibration into the space between a former inserted in the ladle and the ladle wall. After removal of the former, the lining is heated for drying.
- the amount of water for mixing is added with a precision of at least 0.1%, and the moist material is mixed for not more than 4 minutes.
- the lining is heated, preferably to about 150° C., at a maximum rate of 8° C./hour.
- the apparatus comprises a compulsory mixer with a water-metering unit with electrical pulse control for mixing and moistening the dry material, a rotating belt-type conveyor, and a vibration template with one or more vibrators.
- a thixotropic self-curing vibration-compacted refractory material according to the invention with the composition given below in % by weight was used for lining a steel ladle having a capacity of 85 tons:
- amorphous silica having a particle size of less than 1 ⁇ m.
- the fused zirconium silicate/corundum employed had the following composition:
- the bulk density of the fused particles is 3.65 g/cm 3 and the total porosity is 7%.
- the refractory components in the dry state were mixed thoroughly in a mixer, with the addition of (in % by weight)
- the material was packed in plastic big bags.
- the material is free of clay and free of cement and therefore does not contain any crystallisation water.
- the content of free SiO 2 is less than 0.5% by weight.
- the dry material is introduced into a compulsory mixer in batches of 2 tons each and is mixed thoroughly, with the addition of 3.4 kg of water for mixing per 100 kg of dry compound. Exact metering of water is effected by means of electric pulse control, the precision being 0.1%. The mixing time after the addition of water is 4 minutes. The material is then discharged from the mixing apparatus and is transported to the steel ladle to be lined; the introduction of the material into the space between an inserted former and the ladle wall, and the vibration procedure, are carried out within a period of 4 minutes.
- the former is removed.
- the lining is then heated up to 150° C. at a rate of slower than 8° C./hour and than brought to the operating temperature.
- the ready-prepared lining has the following properties:
- a thixotropic self-curing vibration material according to the invention for lining a steel ladle having a capacity of 180 tons, contains the following refractory components:
- ⁇ -alumina having a mean primary particle size of less than 3.5 ⁇ m
- amorphous silica having a particle size of less than 1 ⁇ m.
- the fused zirconium silicate/corundum employed has the following chemical composition (in % by weight): 16% of SiO 2 , 48% of Al 2 O 3 and 36% ZrO.
- the bulk density of the particles is 3.65 g/cm 3 , and the total porosity is 7%.
- the refractory components in the dry state are mixed thoroughly in a compulsory mixer, with the addition of (in % by weight):
- the material is packed in plastic big bags.
- This compound too is clay-free and cement-free.
- the content of free SiO 2 is less than 0.5%.
- the dry material is introduced into a compulsory mixer in batches of 2 tons each and is mixed thoroughly, with the addition of 3.5 kg of water for mixing per 100 kg of dry compound. Exact metering of water is carried out by means of electrical pulse control, the precision being 0.1%. The mixing time after the addition of water is 4 minutes. The compound is then discharged from the mixing apparatus and is transported to the steel ladle to be lined. The introduction of the material into the space between an inserted former and the ladle wall, and the vibration procedure, are carried out within a period of 4 minutes.
- the former is removed.
- the lining is then heated up to 150° C. at a rate of less than 8° C./hour and then brought to the operating temperature.
- the ready-prepared lining has the following properties:
- the drawing shows diagrammatically an embodiment of an apparatus for carrying out the process according to the invention.
- the dry vibration material which is supplied in plastic big bags, is poured into the compulsory mixer 3 via the hopper 4, by means of an overhead crane 2, the compulsory mixer being equipped with a water-metering unit 5.
- the material is mixed thoroughly in the compulsory mixer 3, the amount of water for mixing being added with the aid of the water metering unit 5, with a precision of at least 0.1%.
- the material After the material has been mixed and moistened, it is discharged from the compulsory mixer 3 with the aid of the conveyor belt 6 and is transported into the bunker 8 by means of the inclined lift 7. From the silo 8, the material passes onto a conveyor belt 9, the end of which is equipped with a rotating belt conveyor 10.
- the vibration former 12 with the vibrators 13 is located in the steel ladle 11 to be lined.
- the former 12 rests on an annular rubber cushion 16, while the upper cushioning against a crosshead 14 is effected by means of a plurality of upper and lower rubber cushions 15.
- the crosshead 14 is connected to the ladle by means of fastenings 17.
- the rotating belt conveyor 10 transports the material into the gap between the ladle 11 and the vibration former 12.
- the thixotropix refractory material becomes liquid under vibration and uniformly fills the space between the ladle 11 and the former 12.
- the refractory material becomes solid.
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- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- General Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Composite Materials (AREA)
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- Furnace Housings, Linings, Walls, And Ceilings (AREA)
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Abstract
The invention relates to a thixotropic self-curing refractory material based on zirconium silicate, and a process and an apparatus for lining metallurgical vessels, in particluar ladles in steel plants, with this material which is compacted by means of a vibration method.
Description
This is a continuation, of application Ser. No. 716,898, filed Mar. 28, 1985, now pending.
The property of suitable refractory materials, known as thixotropy whereby the materials become liquid when subjected to vibrations and are converted to a solid state when the vibration ends, is utilised for lining metallurgical vessels with vibration of the lining material.
This lining technique has been introduced into the steel industry for lining tapping spouts in blast furnaces. The thixotropic refractory material is introduced into the tapping spout, caused to flow with the aid of a vibration template, and homogenised and compacted.
This technique has also been used in the foundry industry for lining ladles which are not very high. It has also been proposed to line ladles in steel plants in this manner. In lining ladles in steel plants, however, the lining predominantly used are either linings with refractory bricks or monolithic linings obtained by ramming or slinging refractory compounds. The reason is that the refractory lining of ladles, in which metallurgical treatments of the melt are also frequently carried out today, has to meet high requirements in respect of their durability. The refractory lining of ladles is destroyed predominantly by infiltration and slagging.
The liquid slags and the melt infiltrate the refractory lining, where reactions take place between slags/melt and the refractory material of the lining, these reactions resulting in destruction of the refractory lining. In addition to the refractoriness and the mineral composition, the density of the refractory thixotropic compound used is important with regard to the slag resistance of the refractory lining. Specialists have hitherto apparently been of the opinion that, in the case of ladles in steel plants, an adequate density of the refractory lining cannot be achieved by vibration.
Furthermore, steel ladles which today usually have capacities of from 80 to 320 tons possess linings which are 3 m high or more. With these lining heights, specialists are troubled not only by the problem of an adequate density of the lining, but also by the possibility that the lining which has been subjected to vibration will not itself possess sufficient strength after removal of the template and will collapse.
The compound disclosed as a refractory compound for lining ladles in steel plants is a pourable compound whose principal components are zirconium silicate, a siliceous raw material, for example fireclay, and an alumina binder, the total alumina content of the pourable material being restricted to 5-1.0% by weight (German Auslegeschrift No. 3,235,244, and Nippon Kokan Technical Report, Overseas No. 37, 1983, pages 51 to 53). A disadvantage is the relatively high porosity of 16.5 to 21.5 vol. % and the consequent insufficient slag resistance owing to greater infiltration. Furthermore, as a result of adding fireclay, the lining tends to shrink and is consequently susceptible to fracture. As a result of using an alumina binder, the compound contains water of crystallisation. It also contains free SiO2. This is disadvantageous because SiO2 is reduced in the presence of manganese-containing melts, and siliconisation of the steel occurs.
U.S. Pat. No. 4,292,084 discloses a refractory material for lining metallurgical vessels by vibrating the material to compact it, which can consist of zirconium silicate, tabular alumina, calcined kaolin and phosphoric acid.
These known compounds, however, have bulk densities of only between 2.35 and 2.50 g/cm3. Therefore the slag resistance must be considered insufficient. Because of the high water content of between 6.4 and 7.1%, the lining might collapse after it has been produced by the vibration process and the former has been withdrawn.
It is the object of the present invention to propose a thixotropic self-curing refractory material for vibration compaction with which the stated disadvantages of the known materials can be overcome. In particular, the intention is to improve the infiltration-resistance and slag-repellant action of the lining, as well as its stability under load.
This object is achieved, in accordance with the invention, by a thixotropic self-curing refractory material based on zirconium silicate, and having the following chemical composition (in % by weight):
______________________________________ 24 to 29% SiO.sub.2 10 to 20% Al.sub.2 O.sub.3 0,2 to 0,8% P.sub.2 O.sub.5 0 to 1,5% K.sub.2 O + Na.sub.2 O + LiO.sub.2 0 to 0,5% Fe.sub.2 O.sub.3 0 to 0,05% CaO rest ZrO.sub.2 ______________________________________
It is a main object of the invention to counter the attack by slag on the refractory material and the consequences of this attack, by suitable measures both in terms of the structure (mineralogical composition) and in terms of the texture (density, gas permeability, particle size distribution and porosity). According to the invention the refractory material should preferably have the following crystallographic analysis (in % by weight):
______________________________________
20 to 30% fused zirconium silicate/corundum
1 to 5% alumina
0,1 to 0,5% amorphous silica
0,3 to 1% aluminum metaphosphate
0,5 to 4% alkalisilicate with a molar ratio
of 1:2 to 1:4
rest zirconium silicate
______________________________________
When the molar ratio is greater than 1:2, the alkali metal silicates become too hygroscopic. When the molar ratio is less than 1:4, the alkali metal silicates become water-insoluble. "Molar ratio" is the ratio of the alkali metals to the silicate part of alkali metal silicates.
The zirconium silicate should preferably have the following particle size spectrum:
______________________________________ 1 to 10% 0,001 to 0,01mm 17 to 25% 0,01 to 0,074 mm 65 to 82% 0,074 to 0,5 mm ______________________________________
It is advantageous if a product having the following chemical composition (in % by weight) is used as the fused zirconium silicate/corundum:
______________________________________
13 to 18% SiO.sub.2
32 to 37% ZrO.sub.2
rest Al.sub.2 O.sub.3
______________________________________
The fused product should preferably possess a bulk density of at least 3.60 g/cm3 and a total porosity of 8% or less.
The alumina used should preferably be reactive α-alumina which has a mean primary particle size of less than 3.5 μm and in which at least 45% of the particles have a size of less than 2 μm.
Advantageously, 0.5 to 3% by weight of antioxidants, preferably in the form of aluminum and/or silicon particles, can be added to the material.
It may also be advantageous to add pulverulent wetting agents, preferably alkyl-aryl-polyoxyethanol, which reduce the surface tension of the water for mixing. The amount added is 0.05 to 0.2% by weight.
The amount of water for mixing should be in the range of 2.5 to 3.5 kg per 100 kg of dry compound. A further object of the invention is to propose a suitable process and an apparatus for lining metallurgical vessels, with the thixotropic refractory material according to the invention by a vibration method.
In this process for lining metallurgical vessels, in particular ladles in steel plants, with the new thixotropic self-curing refractory material by a vibration method, the components of the material in the dry state are first mixed thoroughly. Water is added and the wetted material is mixed again. The material is then introduced under continuous vibration into the space between a former inserted in the ladle and the ladle wall. After removal of the former, the lining is heated for drying.
In a preferred embodiment, the amount of water for mixing is added with a precision of at least 0.1%, and the moist material is mixed for not more than 4 minutes.
After removal of the former, the lining is heated, preferably to about 150° C., at a maximum rate of 8° C./hour.
The apparatus according to the invention comprises a compulsory mixer with a water-metering unit with electrical pulse control for mixing and moistening the dry material, a rotating belt-type conveyor, and a vibration template with one or more vibrators.
Advantageously the product has the following particle size spectrum:
______________________________________ 26 to 32% 0 to 0.06 mm 32 to 52% 0.06 to 0.5 mm 23 to 38% as rest 0.5 to 3 mm, ______________________________________
and the zirconium silidale has the following particle size spectrum:
______________________________________ 1 to 10% 0.001 to 0.01mm 17 to 25% 0.01 to 0.074 mm 65 to 82% 0.74 to 0.5 mm. ______________________________________
The invention is illustrated by the following examples.
A thixotropic self-curing vibration-compacted refractory material according to the invention with the composition given below in % by weight was used for lining a steel ladle having a capacity of 85 tons:
36% zirconium silicate having a particle size of up to 0.5 mm,
16% zirconium silicate having a particle size of up to 0.074 mm,
10% zirconium silicate having a particle size between 0.001 and 0.01 mm,
30% fused zirconium silicate/corundum having a particle size of up to 4 mm,
5% α-alumina having a mean primary particle size of less than 3.5 μm and
0.5% amorphous silica having a particle size of less than 1 μm.
The fused zirconium silicate/corundum employed had the following composition:
16% SiO2
48% Al2 O3
36% ZrO2.
The bulk density of the fused particles is 3.65 g/cm3 and the total porosity is 7%.
The refractory components in the dry state were mixed thoroughly in a mixer, with the addition of (in % by weight)
0.5% aluminum metaphosphate powder,
1% sodium silicate having a molar ratio of 1:2.5,
0.5% aluminum powder as an antioxidant, and
0.05% a detergent substance as wetting agent.
The material was packed in plastic big bags.
The chemical analysis of the material is given below (in % by weight):
______________________________________
25% SiO.sub.2
20% Al.sub.2 O.sub.3
0.35% P.sub.2 O.sub.5
0.8% Na.sub.2 O
rest ZrO.sub.2.
______________________________________
The material is free of clay and free of cement and therefore does not contain any crystallisation water. The content of free SiO2 is less than 0.5% by weight.
In a ladle lined with this material, desulphurisation treatments with lime-containing substances can be carried out with improved results, and high-manganese steels can be cast.
In the steel plant, the dry material is introduced into a compulsory mixer in batches of 2 tons each and is mixed thoroughly, with the addition of 3.4 kg of water for mixing per 100 kg of dry compound. Exact metering of water is effected by means of electric pulse control, the precision being 0.1%. The mixing time after the addition of water is 4 minutes. The material is then discharged from the mixing apparatus and is transported to the steel ladle to be lined; the introduction of the material into the space between an inserted former and the ladle wall, and the vibration procedure, are carried out within a period of 4 minutes.
After the vibration procedure, the former is removed. The lining is then heated up to 150° C. at a rate of slower than 8° C./hour and than brought to the operating temperature.
The ready-prepared lining has the following properties:
______________________________________
Vibration density (bulk density):
3.6 g/cm.sup.3
Open porosity: 12 vol. %
Gas permeability: 0.4 nPm
Thermal expansion up to 1.000° C.:
0.4%
Compressive strength in the cold
100 N/mm.sup.2
state after heating to 1.000° C.:
______________________________________
When stainless steel melts were treated in such a lined ladle, the life of the lining corresponded to 78 heats; this is 1.75 times the life of a lining produced using a similar, but rammed, material.
A thixotropic self-curing vibration material according to the invention, for lining a steel ladle having a capacity of 180 tons, contains the following refractory components:
50% by weight of zirconium silicate having a particle size of 0-0.5 mm,
15% by weight of powdered zirconium silicate having a particle size of 0-0.074 mm,
10% by weight of powdered zirconium silicate having a particle size of 0.001-0.01 mm,
20% by weight of fused zirconium silicate/corundum having a particle size of 0-4 mm,
2% by weight of α-alumina having a mean primary particle size of less than 3.5 μm and
0.2% by weight of amorphous silica having a particle size of less than 1 μm.
The fused zirconium silicate/corundum employed has the following chemical composition (in % by weight): 16% of SiO2, 48% of Al2 O3 and 36% ZrO. The bulk density of the particles is 3.65 g/cm3, and the total porosity is 7%.
The refractory components in the dry state are mixed thoroughly in a compulsory mixer, with the addition of (in % by weight):
______________________________________ 0.5% aluminum metaphosphate powder, 1.3% sodium silicate having a molar ratio of 1:3.3, 0.9% aluminum powder as an antioxydant and 0.1% a detergent substance as a wetting agent. ______________________________________
The material is packed in plastic big bags.
The chemical analysis of the material is as follows (in % by weight):
______________________________________
37% SiO.sub.2
13% Al.sub.2 O.sub.3
0.35% P.sub.2 O.sub.5
0.6% Na.sub.2 O
rest ZrO.sub.2
______________________________________
This compound too is clay-free and cement-free. The content of free SiO2 is less than 0.5%.
In the steel plant, the dry material is introduced into a compulsory mixer in batches of 2 tons each and is mixed thoroughly, with the addition of 3.5 kg of water for mixing per 100 kg of dry compound. Exact metering of water is carried out by means of electrical pulse control, the precision being 0.1%. The mixing time after the addition of water is 4 minutes. The compound is then discharged from the mixing apparatus and is transported to the steel ladle to be lined. The introduction of the material into the space between an inserted former and the ladle wall, and the vibration procedure, are carried out within a period of 4 minutes.
After the vibration procedure, the former is removed. The lining is then heated up to 150° C. at a rate of less than 8° C./hour and then brought to the operating temperature.
The ready-prepared lining has the following properties:
______________________________________
Vibration density (bulk density):
3.65 g/cm.sup.3
Open porosity: 11 vol. %
Gas permeability: 0.4 nPm
Thermal expansion at 1000° C.:
0.4%
Compressive strength in the cold
110 N/mm.sup.2.
state after heating to 1000° C.:
______________________________________
When high-grade steel melts were subjected to a treatment comprises desulphurization of the steel, lifetime corresponded to 70 heats. This is 1.2 times the life of a lining produced using a vibrated high-alumina compound of greater porosity.
The drawing shows diagrammatically an embodiment of an apparatus for carrying out the process according to the invention.
The dry vibration material, which is supplied in plastic big bags, is poured into the compulsory mixer 3 via the hopper 4, by means of an overhead crane 2, the compulsory mixer being equipped with a water-metering unit 5. The material is mixed thoroughly in the compulsory mixer 3, the amount of water for mixing being added with the aid of the water metering unit 5, with a precision of at least 0.1%.
After the material has been mixed and moistened, it is discharged from the compulsory mixer 3 with the aid of the conveyor belt 6 and is transported into the bunker 8 by means of the inclined lift 7. From the silo 8, the material passes onto a conveyor belt 9, the end of which is equipped with a rotating belt conveyor 10.
The vibration former 12 with the vibrators 13 is located in the steel ladle 11 to be lined. The former 12 rests on an annular rubber cushion 16, while the upper cushioning against a crosshead 14 is effected by means of a plurality of upper and lower rubber cushions 15.
The crosshead 14 is connected to the ladle by means of fastenings 17. The rotating belt conveyor 10 transports the material into the gap between the ladle 11 and the vibration former 12. When the vibrators 13 are switched on, the thixotropix refractory material becomes liquid under vibration and uniformly fills the space between the ladle 11 and the former 12. When the filling process is completed and the vibrators have been switched off, the refractory material becomes solid.
The heat treatment after removal of the vibration former 12 has been described above in the examples.
Claims (6)
1. A refractory material based on zirconium silicate for lining metallurgical vessels by the vibration method which is free of clay and cement, and on a dry basis consists essentially of the following chemical composition
______________________________________ 24 to 29% SiO.sub.2 10 to 20% Al.sub.2 O.sub.3 0.2 to 0.8% P.sub.2 O.sub.5 maximum 1.5% K.sub.2 O + Na.sub.2 O + LiO.sub.2 maximum 0.5% Fe.sub.2 O.sub.3 maximum 0.05% CaO rest ZrO.sub.2, ______________________________________
having a bulk density of at least 3.6 g/cm3, having the following analysis (in % by weight):
______________________________________
20 to 30% fused zirconium silicate/corundum
1 to 5% alumina
0.1 to 0.5% amorphous silica
0.3 to 1% aluminum metaphosphate
0.5 to 4% alkalisilicate with a molar ratio of
1:2 to 1:4
rest zirconium silicate, and having the
following particle size spectrum:
26 to 32% 0 to 0.06 mm
32 to 52% 0.06 to 0.5 mm
23 to 38% 0.5 to 3 mm,
______________________________________
said material in admixture with water being thixotropic and self-curing.
2. A refractory material based on zirconium silicate for lining metallurgical vessels by the vibration method which is free of clay and cement, and on a dry basis consists essentially of 0.5 to 3% by weight of an antioxidant with the balance consisting essentially of the following chemical composition (in % by weight):
______________________________________ 24 to 29% SiO.sub.2 10 to 20% Al.sub.2 O.sub.3 0.2 to 0.8% P.sub.2 O.sub.5 maximum 1.5% K.sub.2 O + Na.sub.2 O + LiO.sub.2 maximum 0.5% Fe.sub.2 O.sub.3 maximum 0.05% CaO rest ZrO.sub.2, ______________________________________
having a bulk density of at least 3.6 g/cm3, having the following analysis (in % by weight):
______________________________________
20 to 30% fused zirconium silicate/corundum
1 to 5% alumina
0.1 to 0.5% amorphous silica
0.3 to 1% aluminum metaphosphate
0.5 to 4% alkali silicate with a molar ratio
of 1:2 to 1:4
rest zirconium silicate, and
______________________________________
having the following particle size spectrum:
______________________________________ 26 to 32% 0 to 0.06 mm 32 to 52% 0.06 to 0.5 mm 23 to 38% 0.5 to 3 mm, ______________________________________
said material in admixture with water being thixotropic and self-curing.
3. A refractory material based on zirconium silicate for lining metallurgical vessels by the vibration method which is free of clay and cement, and on a dry basis consists essentially of 0.05 to 0.2% by weight of a pulverulent wetting agent with the balance consisting essentially of the following chemical composition (in % by weight):
______________________________________ 24 to 29% SiO.sub.2 10 to 20% Al.sub.2 O.sub.3 0.2 to 0.8% P.sub.2 O.sub.5 maximum 1.5% K.sub.2 O + Na.sub.2 O + LiO.sub.2 maximum 0.5% Fe.sub.2 O.sub.3 maximum 0.05% CaO rest ZrO.sub.2, ______________________________________
having a bulk density of at least 3.6 g/cm3, having the following analysis (in % by weight):
______________________________________
20 to 30% fused zirconium silicate/corundum
1 to 5% alumina
0.1 to 0.5% amorphous silica having a particle
size < 1 um
0.3 to 1% aluminum metaphosphate
0.5 to 4% alkali silicate with a molar ratio
of 1:2 to 1:4
rest zirconium silicate, and
______________________________________
having the following particle size spectrum:
______________________________________ 26 to 32% 0 to 0.06 mm 32 to 52% 0.06 to 0.5 mm 23 to 38% 0.5 to 3 mm, ______________________________________
said material in admixture with water being thixotropic and self-curing.
4. A refractory material according to claim 1, wherein the zirconium silicate has the following particle size spectrum:
______________________________________ 1 to 10% 0.001 to 0.01 mm 17 to 25% 0.01 to 0.074 mm 65 to 82% 0.074 to 0.5 mm. ______________________________________
5. A refractory material according to claim 1, wherein the fused zirconium silicate/corundum has the following chemical composition (in % by weight):
______________________________________
13 to 18% SiO.sub.2
32 to 37% ZrO.sub.2
rest Al.sub.2 O.sub.3
______________________________________
and a total porosity of 8% or less, and the particles possess a bulk density of at least 3.60 g/cm3.
6. A refractory material according to claim 1, wherein the alumina is reactive α-alumina which has a mean primary particle size of less than 3.5 μm and in which at least 45% of the particles are less than 2 μm in size, and the silica used is colloidal silica having a particle size of less than 1 μm.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3445559 | 1984-12-14 | ||
| DE3445559A DE3445559C1 (en) | 1984-12-14 | 1984-12-14 | Refractory, thixotropic vibration mass as well as method and device for the vibration delivery of metallurgical vessels with this mass |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06716898 Continuation | 1985-03-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US4977115A true US4977115A (en) | 1990-12-11 |
Family
ID=6252722
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/902,354 Expired - Fee Related US4977115A (en) | 1984-12-14 | 1986-08-29 | Thixotropic refractory material and a process and apparatus for lining metallurgical vessels with this material by a vibration method |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US4977115A (en) |
| EP (1) | EP0188688B1 (en) |
| CN (1) | CN1017042B (en) |
| AT (1) | ATE52755T1 (en) |
| CA (1) | CA1258683A (en) |
| DD (1) | DD239588A5 (en) |
| DE (2) | DE3445559C1 (en) |
| ES (1) | ES8702320A1 (en) |
| FI (1) | FI854664A7 (en) |
| ZA (1) | ZA858674B (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030015812A1 (en) * | 2001-07-18 | 2003-01-23 | Opatt William M. | Method of installing a refractory lining |
| US6884264B2 (en) | 2001-03-19 | 2005-04-26 | Cambridge Polymer Group, Inc. | System and methods for reducing interfacial porosity in cements |
| CN102773906A (en) * | 2012-07-09 | 2012-11-14 | 郑州东方安彩耐火材料有限公司 | Corundum sand mold for producing fused-cast alumina refractory materials and production technique thereof |
| CN103692537A (en) * | 2013-12-14 | 2014-04-02 | 郑州东方安彩耐火材料有限公司 | Casting mould for hanging wall bricks, and preparation technology thereof |
| US20140165573A1 (en) * | 2011-08-31 | 2014-06-19 | Siemens Aktiengesellschaft | Process for producing refractory ceramics for gas turbine plants |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102012113074A1 (en) | 2012-12-22 | 2014-07-10 | Ask Chemicals Gmbh | Mixtures of molding materials containing metal oxides of aluminum and zirconium in particulate form |
| CN115448703B (en) * | 2022-09-06 | 2023-05-19 | 宜兴市隆昌耐火材料有限公司 | Preparation method of high-temperature wear-resistant castable containing zirconia-corundum |
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- 1984-12-14 DE DE3445559A patent/DE3445559C1/en not_active Expired
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- 1985-11-15 DE DE8585114512T patent/DE3577691D1/en not_active Expired - Fee Related
- 1985-11-15 AT AT85114512T patent/ATE52755T1/en not_active IP Right Cessation
- 1985-11-15 EP EP85114512A patent/EP0188688B1/en not_active Expired - Lifetime
- 1985-11-26 FI FI854664A patent/FI854664A7/en not_active Application Discontinuation
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6884264B2 (en) | 2001-03-19 | 2005-04-26 | Cambridge Polymer Group, Inc. | System and methods for reducing interfacial porosity in cements |
| US20030015812A1 (en) * | 2001-07-18 | 2003-01-23 | Opatt William M. | Method of installing a refractory lining |
| WO2003008889A1 (en) * | 2001-07-18 | 2003-01-30 | Allied Mineral Products, Inc. | Method of installing a refractory lining |
| US6743382B2 (en) | 2001-07-18 | 2004-06-01 | Allied Mineral Products, Inc. | Method of installing a refractory lining |
| US20140165573A1 (en) * | 2011-08-31 | 2014-06-19 | Siemens Aktiengesellschaft | Process for producing refractory ceramics for gas turbine plants |
| CN102773906A (en) * | 2012-07-09 | 2012-11-14 | 郑州东方安彩耐火材料有限公司 | Corundum sand mold for producing fused-cast alumina refractory materials and production technique thereof |
| CN103692537A (en) * | 2013-12-14 | 2014-04-02 | 郑州东方安彩耐火材料有限公司 | Casting mould for hanging wall bricks, and preparation technology thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN85108841A (en) | 1986-06-10 |
| EP0188688B1 (en) | 1990-05-16 |
| DD239588A5 (en) | 1986-10-01 |
| FI854664A7 (en) | 1986-06-15 |
| CA1258683A (en) | 1989-08-22 |
| FI854664A0 (en) | 1985-11-26 |
| ZA858674B (en) | 1986-07-30 |
| DE3577691D1 (en) | 1990-06-21 |
| ES549897A0 (en) | 1987-01-01 |
| DE3445559C1 (en) | 1986-08-14 |
| ATE52755T1 (en) | 1990-06-15 |
| ES8702320A1 (en) | 1987-01-01 |
| CN1017042B (en) | 1992-06-17 |
| EP0188688A3 (en) | 1987-12-02 |
| EP0188688A2 (en) | 1986-07-30 |
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